That's awesome! Congratulations.

Thanks for your input! You’re absolutely right. Internal asymmetric alkynes often produce a mixture of ketones, making the last step less selective. This can result in lower yields of the target molecule. Separating the target product typically requires additional steps, like chromatography. While this is a limitation of the method shown, it’s a realistic challenge in organic synthesis and highlights the complexity of achieving high selectivity. In future content, I’ll explore strategies to address such issues. Your feedback is invaluable!

Thank you 😊

@favormaybel7768 Thank you, Menye. So good to see you here.

No worries at all, it happens!🙂

Hi, I'm glad you watched the video to the end, and you do have a valid point. Although I meant for the triple bonds to be longer than that, with no gaps, it should be between carbon one and two as I labeled. But if we assume that the gap is an additional carbon as per your observation (note that usually the gap will be a bit more prominent than this), then it means we have a total of 7 parent carbons, and that will be 4,5-dimethylhept-1-yne instead. I'm glad you picked it up. You have great eyes for details. Bravo 👏. I will make sure not to create such confusion in my subsequent videos. Thank you.

Hello, example two is a terminal alkene, not a ketone. A ketone will have oxygen attached to the carbon double bond. I hope this clears it up for you.

Thank you sis

Glad I could help! And thanks for your feedback and subscription that motivates me to do more videos.

@@joyoyebisitutoring Yes ma'am 'always give in more as much as you can... 💝🤝✍

Okay noted

Ok noted.👍